Acute zonal occult outer retinopathy in a patient with retinitis pigmentosa.

Ekaterina Milovanova, Michael P Fielden, Faazil Kassam
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Abstract

A 30-year-old woman with a phenotypic presentation of retinitis pigmentosa (RP) presented with a 5-day history of painless, acute vision loss in her right eye, with visual acuity dropping from 20/30 to hand motions. Optical coherence tomography of the right macula showed near-complete loss of the ellipsoid layer. Treatment with a prolonged course of oral prednisone resulted in a complete structural regeneration of the ellipsoid layer and improvement of visual acuity to 20/50, with eccentric fixation. Tests for infectious diseases, autoimmune disorders, and rare RP mimic syndromes (eg, Refsum disease) were negative. The patient has remained stable since. We favor a diagnosis of two separate pathologies and suggest a designation of acute zonal occult outer retinopathy (AZOOR) in RP for this previously unreported presentation.

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色素性视网膜炎患者的急性区域性隐匿性外视网膜病变。
一名30岁女性,表型表现为视网膜色素变性(RP),右眼无痛性急性视力丧失5天,视力从20/30下降到手部运动。右侧黄斑的光学相干断层扫描显示椭球层几乎完全消失。延长疗程的口服强的松治疗导致椭球层结构完全再生,视力改善至20/50,偏心固定。传染病、自身免疫性疾病和罕见的RP模拟综合征(如Refsum病)的检测均为阴性。此后病人病情一直稳定。我们倾向于诊断两种不同的病理,并建议在RP中指定急性区域性隐匿性外视网膜病变(AZOOR)。
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来源期刊
Digital journal of ophthalmology : DJO
Digital journal of ophthalmology : DJO Medicine-Medicine (all)
CiteScore
0.80
自引率
0.00%
发文量
14
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